Current Bioactive Compounds最新文献

{"title":"Role of Sapindus emarginatus Pericarp Extract in Gut Serotonin Level and its Emetic Activity in Animal Models","authors":"L. Vivekanandan, Prabha Thangavelu, Jagadeeswaran Murugesan, Hemalatha Selvaraj","doi":"10.2174/1573407219666230815121205","DOIUrl":"https://doi.org/10.2174/1573407219666230815121205","url":null,"abstract":"\u0000\u0000Emesis is a complexand distressing protective mechanism that helps to remove toxic substances from the stomach and prevent further ingestion. The emetics and cathartics are predominantly used for accidental and intentional ingestion of poisons or toxins. The availability and usage of emetics in humans are limited because of their side effects. Therefore, to treat poisoned people, we need effective medications. Sapindus emarginatus Vahl., often called soapnut, is a member of the Sapindaceae family. They have historically been used as emetic, antipruritic, laxative, antifertility, and anti-inflammatory medicines.\u0000\u0000\u0000\u0000This study aims to assess the gut serotonin level and emetic effect of Sapindus emarginatus hydroethanolic pericarp extract (HESE) by using animal models.\u0000\u0000\u0000\u0000Gravimetric analysis was used to determine the HESE's saponin content. The emetic effect of the HESE at a dose of 250, 500, 1000, and 2000 mg/kg was evaluated by copper sulfate-induced emesis in the chick model and cisplatin-induced emesis in the rat-pica model. The serotonin level in rat intestinal mucosa was measured by spectrofluorimetry.\u0000\u0000\u0000\u0000HESE was estimated to contain 11.92% saponin. The extract at high doses of 1000 and 2000 mg/kg showed emetic activity evidenced by increased frequency of retching in chick, increased kaolin intake, and anorexia in the rat-pica model. The extract showed a significant increase in serotonin levels in the proximal part of the small intestine in comparison with normal animals.\u0000\u0000\u0000\u0000According to the results of the current investigation, which employed various animal models, the HESE demonstrated appreciable emetic activity. The extract at a high dose showed a significant emetic effect due to increased serotonin levels in the gut. The HESE was discovered to be a strong contender for the treatment of poisoned patients. More research are required to validate their adverse effects of frequent usage.\u0000","PeriodicalId":10772,"journal":{"name":"Current Bioactive Compounds","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-08-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"43003641","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Synthesis of New Glycosylamine Derivatives based on Carbohydrates","authors":"H. Jabbari","doi":"10.2174/1573407219666230810094657","DOIUrl":"https://doi.org/10.2174/1573407219666230810094657","url":null,"abstract":"\u0000\u0000Glycosylamine play an important role in living organisms. Most plants\u0000store their chemical resources in the form of inactive glycosides, which are broken down and\u0000converted into sugar in the body of herbivores by hydrolyzing enzymes. Glycosylamine are\u0000obtained from the secondary metabolism of plants and consist of two parts. One part of it contains\u0000sugar like glucose and is inactive in most substances, and has a good effect on the solubility of the\u0000glycosylamine derivatives and its absorption and even its transfer from one organ to another. The\u0000therapeutic effect is related to the second part, which is called aglycan (or aglucan). Glycosylamine\u0000derivatives form a large group of valuable medicinal substances, which at the same time include\u0000some of the most dangerous and toxic substances in nature. These substances are present in many\u0000groups of flowering plants. Glycosides are made in different ways in different metabolic pathways.\u0000These materials have a complex and special chemical structure and leave special effects on the\u0000human body. Glycosylamine derivatives are called O-glycosid, N-glycosid, S-glycosid in terms of\u0000atoms coupling to anomeric carbon. Carbohydrate esterification reaction to prepare new glycosylamine derivatives is one of the most important carbohydrate reactions. The anomeric position of\u0000carbohydrates with strong leaving groups is very important for the preparation of glycosides.\u0000Preparation of glycosylamine derivatives based on acetylated carbohydrates is the main purpose of this\u0000article. Different carbohydrates were acetylated under mild conditions and high yields. The anomeric\u0000position was deacetylated by a magnesium oxide heterogeneous catalyst in methanol solvent. In order\u0000to prepare new glycosides acetylated/ deacytylated carbohydrate reacted with N-Methyl-(naphtha-2-\u0000ylmethoxy)amine. The final product was identified by various spectroscopic methods.\u0000\u0000\u0000\u0000Anhydrous sodium acetate (4 g) and α-D-glucose (28 mg, 5 g) were mixed. The mixture\u0000was transferred to a 200 ml Round-bottom flask . Acetic acid (260 mg, 25 ml) was added to the\u0000reaction mixture. The reaction mixture was heated in a boiling water bath for 2 h until complete\u0000dissolution of the glucose. Then 100 ml of ice was added. After 1 hour, White crystals formed and\u0000were washed with cold water. And then 1 mol of glucose pentaacetate per 50 ml of methanol was\u0000dissolved by a magnetic stirrer. After thatMgO (0.2gr) was added to the reaction mixture. The\u0000reaction mixture was refluxed at room temperature within 4-5 hours. After 5 hours, the solvent was\u0000removed and separated by chromatography. It is then washed with hexane and crystallized by etherhexane. And the final step reacted with N-Methyl- (naphtha-2-ylmethoxy) amine in order to prepare\u0000new glycosylamine derivatives.\u0000\u0000\u0000\u0000Magnesium oxide in methanol solvent is one of the best effective catalysts in the\u0000deacetylation of the anomer position of acetylated carbohydrates. It is done under ambient temperature\u0000and in very easy","PeriodicalId":10772,"journal":{"name":"Current Bioactive Compounds","volume":"1 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-08-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"41407933","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"The Inefficiency of Low-concentration Curcumin Intervention in Ameliorating\u0000Chronic-stage Pulmonary Fibrosis","authors":"F. Muneesa M, Y. Bhandary","doi":"10.2174/1573407219666230810094839","DOIUrl":"https://doi.org/10.2174/1573407219666230810094839","url":null,"abstract":"\u0000\u0000Curcumin, a polyphenol compound, is reported to exhibit ameliorative\u0000effects in acute lung injury and different organ fibrosis models. We have previously demonstrated\u0000that curcumin, at a dose of 75 mg/kg, could modulate inflammatory mediators and fibrinolytic system proteins in the inflammatory stage as well as fibroproliferative stage in a mouse model of bleomycin (BLM) induced pulmonary fibrosis. In this study, we investigated the efficacy of the same\u0000dose of curcumin in resolving the established fibrotic stage in a mouse model of BLM-induced\u0000pulmonary fibrosis.\u0000\u0000\u0000\u0000We prepared the fibrosis model by intranasal administration of BLM (2 mg/kg). Curcumin intervention was performed by intraperitoneal injection on 16th to 20th days post BLM exposure. The control group was administered with normal saline. The mice were sacrificed on the 21st\u0000day post BLM exposure.\u0000\u0000\u0000\u0000Histological analysis of the lung tissue samples indicated that curcumin (75 mg/kg) could\u0000not reverse the fibrotic features induced by BLM. We also performed RT-PCR and western blot to\u0000examine the molecular changes induced by BLM and curcumin. It was observed that curcumin\u0000could neither reduce the expressions of fibrotic markers nor restore the normal expressions of proteins in the fibrinolytic system.\u0000\u0000\u0000\u0000Our data suggest that a low dose of curcumin is not effective in ameliorating the fibrotic stage of BLM-induced pulmonary fibrosis. An increased dose or a formulation that increases\u0000the bioavailability of curcumin could probably exhibit promising effects against pulmonary fibrosis\u0000in the future.\u0000","PeriodicalId":10772,"journal":{"name":"Current Bioactive Compounds","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-08-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"45879288","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"A Critical Review Based on Preclinical Studies of Medicinal Plants for the\u0000Management of Alzheimer’s Disease","authors":"Swati Wadhawan, Vishal Kumar Biswkarma, A. Chaudhary, Priya Masand","doi":"10.2174/1573407219666230807150426","DOIUrl":"https://doi.org/10.2174/1573407219666230807150426","url":null,"abstract":"\u0000\u0000Alzheimer’s disease (AD) is the most common neurodegenerative and progressive disorder that results in damage to memory and alters thinking and behavior, which represent critical\u0000problems the world’s aging population is faced with. Clinical symptoms of AD include cognitive\u0000decline, loss of memory, emotional and behavioral changes, loss of motor coordination, and mental\u0000impairments. Yet, neither a universally accepted diagnosis with respect to its pathogenesis nor an\u0000ideal therapy is available for the management of AD. The existing drugs cause many complications\u0000and adverse effects. Herbal drugs, supported by an abundance of traditional knowledge, may fulfill\u0000the need as they can target the pathogenesis of AD at various destinations, both at the cellular and\u0000molecular levels. In recent years, herbal drugs and formulations have been evaluated in preclinical\u0000setups, especially involving rat and mouse models of AD, which have shown their memoryenhancing, neuroprotective, and antioxidant activities. Several herbal drugs and phytochemicals\u0000have been evaluated for their effectiveness as antioxidative agents to prevent the occurrence of oxidative stress and ROS formation during AD pathogenesis and exhibit antiapoptotic properties by\u0000downregulating caspase-3, DNA fragmentation, NF-κB, interleukin-1 β (IL1β), and TNF levels. In\u0000this paper, we have primarily reviewed herbal remedies that have been recently evaluated as alternative treatments for AD in a preclinical setup, and discussed the role of herbal medicines in the\u0000management of AD and advances in their knowledge.\u0000","PeriodicalId":10772,"journal":{"name":"Current Bioactive Compounds","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-08-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"47555651","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Impact of Phytomolecules with Nanotechnology on the Treatment of\u0000Inflammation","authors":"Sonia Singh, Bhupesh C. Semwal, Himanshu Sharma, D. Sharma","doi":"10.2174/1573407219666230807150030","DOIUrl":"https://doi.org/10.2174/1573407219666230807150030","url":null,"abstract":"\u0000\u0000Inflammation is a part of the biological response of body tissues against harmful stimuli,\u0000such as damaged cells, pathogens, irradiations, and toxic compounds. Numerous treatments, including anti-inflammatory drugs that treat the condition of inflammation, are available for its management. Because of the severe adverse effects associated with synthetic medications, phytotherapy\u0000may be a promising and effective approach to treating inflammation. The therapeutic potential of\u0000herbs is due to their capacity to target a variety of inflammatory mediators, including chemokines,\u0000cytokines, nitric oxide, lipoxygenase, nuclear factor kappa-B, and arachidonic acid. Furthermore,\u0000nanomedicine may be a valuable and effective formulation approach for overcoming the drawbacks\u0000of phytoconstituents, such as their low bioavailability, high first-pass metabolism, and poor stability. The current manuscript provides a thorough description of many phytoconstituents and herbal\u0000plants that have great potential for treating inflammation-related diseases, as well as information on\u0000their limitations, drug formulations, and regulatory issues.\u0000","PeriodicalId":10772,"journal":{"name":"Current Bioactive Compounds","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-08-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"47741183","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Meet the Editorial Board Member","authors":"Marcello Locatelli","doi":"10.2174/157340721907230706115540","DOIUrl":"https://doi.org/10.2174/157340721907230706115540","url":null,"abstract":"","PeriodicalId":10772,"journal":{"name":"Current Bioactive Compounds","volume":"52 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"135771258","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Anti-Inflammatory Potential of Curcumin: From Chemistry and Mechanistic Insight to Nanoformulations","authors":"H. Tuli, D. Aggarwal, M. Chaudhary, Nandini Bajaj, Deepika Sharma, S. Upadhyay, V. Garg, H. Abdulabbas, Isha Rani","doi":"10.2174/1573407219666230726164538","DOIUrl":"https://doi.org/10.2174/1573407219666230726164538","url":null,"abstract":"\u0000\u0000Curcumin is a natural compound obtained from Curcuma longa that possesses a vast therapeutic potential for disease treatment. It is a potent anticancer, anti-inflammatory, antioxidant, and anti-aging phytochemical as evident from numerous studies. Curcumin's anti-inflammatory and antioxidant properties are thought to be more potent than its other biological actions. Curcumin's anti-inflammatory properties can lead to an improvement in symptoms and make it a viable candidate for the treatment and prevention of pro-inflammatory disorders.\u0000\u0000\u0000\u0000The goal of this review is to analyse curcumin's anti-inflammatory properties and mechanisms in the treatment of various disorders. The effect of different curcumin-based nanoformulations on anti-inflammatory potential is also reviewed, as the therapeutic use of curcumin is influenced by its solubility, bioavailability, and pharmacokinetic profile.\u0000\u0000\u0000\u0000The literature searched during the last ten years using keywords such as curcumin, anti-inflammatory mechanisms, cytokines, and nanoformulations from multiple databases, such as PubMed, Science Direct, Scopus, and others. The quality research and review articles containing the aforementioned keywords were chosen for this review article.\u0000\u0000\u0000\u0000This review focuses on the anti-inflammatory properties of curcumin against a variety of inflammatory disorders that arise over the course of various illnesses. It also emphasises the importance of developing alternative nanoformulations to address the limitations of curcumin usage. Further, it will aid the scientific community's understanding of curcumin and its anti-inflammatory mechanisms, prompting them to devise innovative treatment options.\u0000","PeriodicalId":10772,"journal":{"name":"Current Bioactive Compounds","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-07-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"49132602","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Antioxidant, Antibacterial, α-Amylase, and α-Glucosidase Inhibition, and Anti-inflammatory Activities of Mimosa rubicaulis Lam","authors":"A. Adhikari, D. Shrestha, Sushma Thapa, Tamlal Pokhrel, Bishnu Bahadur Sinjali, J. Baral","doi":"10.2174/1573407219666230720103734","DOIUrl":"https://doi.org/10.2174/1573407219666230720103734","url":null,"abstract":"\u0000\u0000The use of medicinal plants as supplemental or alternative medicine is widespread around the world. For the development of new drugs, studies on these medicinal plants that include pharmacological and toxicological assessments are crucial.\u0000\u0000\u0000\u0000This work aimed to find the total phenolic and flavonoid content, antioxidant, antibacterial, and antidiabetic potential of the traditionally used medicinal plant Mimosa rubicaulis Lam.\u0000\u0000\u0000\u0000The in vitro antidiabetic potential of methanolic extract and its fractions of the roots of M. rubicaulis were performed via enzyme (α-glucosidase and α-amylase) inhibition assays. Antioxidant and anti-inflammatory activities were carried out using 2,2 Diphenyl-1-picrylhydrazyl (DPPH), and reactive oxygen species (ROS) inhibiting methods. Well diffusion method is applied for antibacterial activity. Autodock vina was used for molecular docking.\u0000\u0000\u0000\u0000The crude extract reported the highest inhibition activity against α-glucosidase with an IC50 value of 10.29 ± 0.35 μg/mL compared to the standard acarbose IC50 value of 5.653 ± 0.29 µg/mL. Similarly, the ethyl acetate (EA) fraction disclosed significant inhibition against α-amylase with an IC50 value of 108.7 ± 0.66 μg/mL compared to the standard drug’s IC50 value of 6.01 ± 0.14 µg/mL. Likewise, the EA fraction showed the maximum antioxidant activity with an IC50 value of 11.89 ± 1.05μg/mL among the crude extract and its fractions.\u0000\u0000\u0000\u0000Mimosa rubicaulis was found to have α-glucosidase and α-amylase inhibition, anti-inflammatory, and antibacterial activity. To the best of our knowledge, this is the first report of α-glucosidase and α-amylase inhibition activity of this plant. Further studies on this plant are required to isolate potent compounds.\u0000","PeriodicalId":10772,"journal":{"name":"Current Bioactive Compounds","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-07-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"43426010","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Optimization of Antioxidant and Antimicrobial Activities by Fractionation of Artemisia judaica subsp. sahariensis Crude Extract from Ahaggar (Algerian Arid Region): UPLC-ESI-MS/MS Analysis of Fractions","authors":"R. Kebbab, Aida basseddik, Walid Boussebaa, E. Nabti, K. Houali","doi":"10.2174/1573407219666230718125630","DOIUrl":"https://doi.org/10.2174/1573407219666230718125630","url":null,"abstract":"\u0000\u0000In recent years, medicinal plants have received considerable attention due to the search for novel bioactive compounds. In this optic, we have been interested in Artemisia judaica subsp. Sahariensis, a Saharan species widely used in phytotherapy by the Tuaregs of the Ahaggar.\u0000\u0000\u0000\u0000This study aims to evaluate and optimize the biological activities of this plant in order to valorize its bioactive compounds.\u0000\u0000\u0000\u0000For this purpose, an extraction with methanol (70%) was carried out, then a liquid-liquid fractionation, using solvents with increasing polarity: diethyl ether, ethyl acetate, n-butanol and water. We realized an analysis of phenols, flavonoids and evaluation of antioxidant and antimicrobial activities in addition to the UPLC-ESI-MS/MS analysis of the fractions.\u0000\u0000\u0000\u0000The reducing effect was proportional to the solvent polarity. The crude extract gave the best reducing power (17.55±3.06µg/mL), better phenols and flavonoids contents (20.35±0.5 mgGAE/gTDM), (10.35±0.56 mgGAE/gTDM) respectively compared to its fractions. The DPPH (2,2-Diphenyl-1-Picrylhydrazyl) radical scavenging assay showed that the ethyl acetate fraction was the most active with the lowest IC50 value (inhibitory concentration to 50% of DPPH) (41.43±0.24 µg/ml) followed by n-butanol (58.53±0.20 µg/mL), diethyl ether (135.07±6.18 µg/mL) and aqueous (226.41±1.51 µg/mL) fractions (p<0.0001). Moreover, hydromethanolic extract gave an IC50 value of 114.05±3.37 µg/mL. The antimicrobial effect was observed on all clinical multi-resistant bacteria tested except Klebsiella pneumoniae, which was resistant. The most important effect was observed by the ethyl acetate fraction against the fungal strain Candida albicans. Various phenolic acids and flavonoids (flavones, flavonols, flavanones) were detected and could be responsible for these bioactivities.\u0000\u0000\u0000\u0000We can conclude that liquid-liquid extraction with solvents of increasing polarity plays a major role in optimizing the biological activity of this plant, which contains polyphenols and can therefore be valued as a source of natural antioxidants and antimicrobials.\u0000","PeriodicalId":10772,"journal":{"name":"Current Bioactive Compounds","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-07-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"49507240","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"A profound insight into the structural modification of natural bioactive compounds containing piperazine moiety: a comprehensive review..","authors":"B. Chopra, N. Saini, Ashwani Kumar Dhingra","doi":"10.2174/1573407219666230718105347","DOIUrl":"https://doi.org/10.2174/1573407219666230718105347","url":null,"abstract":"\u0000\u0000Piperazine is the heterocyclic nucleus and exhibits significant biological potential such as antipsychotic, antidepressant, antihistamine, anticancer, anti-anginal, cardioprotective, antiviral, and anti-inflammatory activity. As a result, it had been considered a crucial structural component in the majority of the therapeutic medications that were already on the market. Other issues that limit its use include solubility, limited bioavailability, cost-effectiveness, and a mismatch between the drug's pharmacokinetic and pharmacodynamic profiles. Literature describes structural modification in the piperazine moiety to create novel derivatives or analogues to solve the issues with currently marketed medications. Nature provides various bioactive components having piperazine nuclei in their core structure. The present review describes the potential of the piperazine nucleus present in natural bioactive components. So the study concludes that it is vital to concentrate on the structural characteristics of this scaffold, which opens the way for future research and may benefit pharmaceutical companies as well as medicinal chemists.\u0000","PeriodicalId":10772,"journal":{"name":"Current Bioactive Compounds","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-07-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"44001340","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}